Colapinto Patricio, Sheth Hiten G, Jain Rajni, Joshi Naresh, Wong Tina
Department of Ophthalmology, Chelsea & Westminster Hospital, London, UK.
Orbit. 2007 Dec;26(4):287-9. doi: 10.1080/01676830601174585.
Orbital schwannoma accounts for less than 5% of orbital tumours and few cases arising in the superior orbit are reported in the literature.
To present, to our knowledge, the first report of inferior oblique-associated orbital schwannoma.
Interventional case report with clinical photographs, MRI imaging, intra-operative photographs and histology.
A 68 year-old man presented with decreased right vision and double vision in downgaze. Examination revealed a right 3 mm ptosis, hypertropia and limitation of depression. Exploration and excision, via anterior orbitotomy, and histological examination confirmed a schwannoma located within the right inferior oblique muscle. Vision normalised post-operatively and there has been no clinical or radiological recurrence of the lesion at 2 years.
This rare case highlights that schwannoma may occur in association with the inferior oblique complex and we suggest that schwannomas should now be considered in the differential diagnosis when patients present with a clinically-suspected or radiologically-proven orbital mass.
眼眶神经鞘瘤占眼眶肿瘤的比例不到5%,文献中报道的起源于眶上的病例很少。
据我们所知,本文首次报道了与下斜肌相关的眼眶神经鞘瘤。
采用介入病例报告,并附临床照片、MRI成像、术中照片和组织学检查。
一名68岁男性患者出现右眼视力下降及向下注视时复视。检查发现右眼上睑下垂3mm,上斜视,下转受限。经前路眶切开术进行探查和切除,并经组织学检查证实神经鞘瘤位于右下斜肌内。术后视力恢复正常,2年时病变无临床及影像学复发。
这一罕见病例表明神经鞘瘤可能与下斜肌复合体相关,我们建议当患者出现临床怀疑或影像学证实的眼眶肿物时,神经鞘瘤应纳入鉴别诊断。